E75.2

Other sphingolipidosis

Coding guidance (WHO 2019)

Disease: Fabry(-Anderson) Gaucher Krabbe Niemann-Pick Farber syndrome Metachromatic leukodystrophy Sulfatase deficiency Excl.: adrenoleukodystrophy [Addison-Schilder] (E71.3)

Sibling codes

E75Disorders of sphingolipid metabolism and other lipid storage disorders E75.0GM2 gangliosidosis E75.1Other gangliosidosis E75.3Sphingolipidosis, unspecified E75.4Neuronal ceroid lipofuscinosis E75.5Other lipid storage disorders E75.6Lipid storage disorder, unspecified